Canonical Allele Identifier: CA7649009
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 570401
dbSNP Id: rs761507884

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323575C>T , CM000677.2:g.73323575C>T GRCh38
NC_000015.9:g.73615916C>T , CM000677.1:g.73615916C>T GRCh37
NC_000015.8:g.71402969C>T NCBI36
NG_009063.1:g.50690G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2518G>A MANE Select ENSP00000261917.3:p.Ala840Thr
ENST00000261917.3:c.2518G>A ENSP00000261917.3:p.Ala840Thr
NM_005477.2:c.2518G>A NP_005468.1:p.Ala840Thr
XM_011521148.1:c.1300G>A XP_011519450.1:p.Ala434Thr
XM_011521148.2:c.1300G>A XP_011519450.1:p.Ala434Thr
NM_005477.3:c.2518G>A MANE Select NP_005468.1:p.Ala840Thr